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263769-03-5

methyl 4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-hydroxybutanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

263769-03-5

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263769-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 263769-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,7,6 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 263769-03:
(8*2)+(7*6)+(6*3)+(5*7)+(4*6)+(3*9)+(2*0)+(1*3)=165
165 % 10 = 5
So 263769-03-5 is a valid CAS Registry Number.

263769-03-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-hydroxybutanoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:263769-03-5 SDS

263769-03-5Downstream Products

263769-03-5Relevant articles and documents

Carbonylative ring opening of terminal epoxides at atmospheric pressure

Denmark, Scott E.,Ahmad, Moballigh

, p. 9630 - 9634 (2007)

(Chemical Equation Presented) The carbonylative opening of terminal epoxides under mild conditions has been developed using Co2-(CO) 8 as the catalyst. Under 1 atm of carbon monoxide and at room temperature in methanol, propylene oxide is converted to methyl 3-hydroxybutanoate in up to 89% yield. This transformation is general for many terminal epoxides bearing alkyl, alkenyl, aryl, alkoxy, chloromethyl, phthalimido, and acetal functional groups. The opening takes place without epimerization at the secondary stereocenter.

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